Long-Term Physical (In)Stability of Spray-Dried Amorphous Drugs: Relationship with Glass-Forming Ability and Physicochemical Properties

被引:22
作者
Edueng, Khadijah [1 ,2 ]
Bergstrom, Christel A. S. [1 ]
Grasjo, Johan [1 ]
Mahlin, Denny [1 ,3 ]
机构
[1] Uppsala Univ, Dept Pharm, Husargatan 3, S-75123 Uppsala, Sweden
[2] Int Islamic Univ Malaysia, Kulliyyah Pharm, Jalan Istana, Bandar Indera Mahkota 25200, Kuantan Pahang, Malaysia
[3] AstraZeneca, S-15185 Sodertalje, Sweden
基金
瑞典研究理事会; 欧洲研究理事会;
关键词
long-term stability; amorphous; glass-forming ability; glass stability; physicochemical properties; crystallization; spray-drying; humidity; melt-quenching; CRYSTALLIZATION TENDENCY; TRANSITION TEMPERATURE; STABILITY; PREDICTIONS; STATE; WATER; CLASSIFICATION; DISSOLUTION; SELECTION; MOBILITY;
D O I
10.3390/pharmaceutics11090425
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study shows the importance of the chosen method for assessing the glass-forming ability (GFA) and glass stability (GS) of a drug compound. Traditionally, GFA and GS are established using in situ melt-quenching in a differential scanning calorimeter. In this study, we included 26 structurally diverse glass-forming drugs (i) to compare the GFA class when the model drugs were produced by spray-drying with that when melt-quenching was used, (ii) to investigate the long-term physical stability of the resulting amorphous solids, and (iii) to investigate the relationship between physicochemical properties and the GFA of spray-dried solids and their long-term physical stability. The spray-dried solids were exposed to dry (<5% RH) and humid (75% RH) conditions for six months at 25 degrees C. The crystallization of the spray-dried solids under these conditions was monitored using a combination of solid-state characterization techniques including differential scanning calorimetry, Raman spectroscopy, and powder X-ray diffraction. The GFA/GS class assignment for 85% of the model compounds was method-dependent, with significant differences between spray-drying and melt-quenching methods. The long-term physical stability under dry condition of the compounds was predictable from GFA/GS classification and glass transition and crystallization temperatures. However, the stability upon storage at 75% RH could not be predicted from the same data. There was no strong correlation between the physicochemical properties explored and the GFA class or long-term physical stability. However, there was a slight tendency for compounds with a relatively larger molecular weight, higher glass transition temperature, higher crystallization temperature, higher melting point and higher reduced glass transition temperature to have better GFA and better physical stability. In contrast, a high heat of fusion and entropy of fusion seemed to have a negative impact on the GFA and physical stability of our dataset.
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页数:20
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  • [1] Physical stability of drugs after storage above and below the glass transition temperature: Relationship to glass-forming ability
    Alhalaweh, Amjad
    Alzghoul, Ahmad
    Mahlin, Denny
    Bergstrom, Christel A. S.
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 495 (01) : 312 - 317
  • [2] Computational Predictions of Glass-Forming Ability and Crystallization Tendency of Drug Molecules
    Alhalaweh, Amjad
    Alzghoul, Ahmad
    Kaialy, Waseem
    Mahlin, Denny
    Bergstrom, Christel A. S.
    [J]. MOLECULAR PHARMACEUTICS, 2014, 11 (09) : 3123 - 3132
  • [3] Role of Viscosity in Influencing the Glass-Forming Ability of Organic Molecules from the Undercooled Melt State
    Baird, Jared A.
    Santiago-Quinonez, Darlene
    Rinaldi, Carlos
    Taylor, Lynne S.
    [J]. PHARMACEUTICAL RESEARCH, 2012, 29 (01) : 271 - 284
  • [4] A Classification System to Assess the Crystallization Tendency of Organic Molecules from Undercooled Melts
    Baird, Jared A.
    Van Eerdenbrugh, Bernard
    Taylor, Lynne S.
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (09) : 3787 - 3806
  • [5] Glass Forming Ability of Amorphous Drugs Investigated by Continuous Cooling and Isothermal Transformation
    Blaabjerg, Lasse I.
    Lindenberg, Eleanor
    Lobmann, Korbinian
    Grohganz, Holger
    Rades, Thomas
    [J]. MOLECULAR PHARMACEUTICS, 2016, 13 (09) : 3318 - 3325
  • [6] Influence of preparation pathway on the glass forming ability
    Blaabjerg, Lasse Ingerslev
    Lindenberg, Eleanor
    Rades, Thomas
    Grohganz, Holger
    Lobmann, Korbinian
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 521 (1-2) : 232 - 238
  • [7] Assessment of crystalline disorder in cryo-milled samples of indomethacin using atomic pair-wise distribution functions
    Botker, Johan P.
    Karmwar, Pranav
    Strachan, Clare J.
    Cornett, Claus
    Tian, Fang
    Zujovic, Zoran
    Rantanen, Jukka
    Rades, Thomas
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 417 (1-2) : 112 - 119
  • [8] The Need for Restructuring the Disordered Science of Amorphous Drug Formulations
    Edueng, Khadijah
    Mahlin, Denny
    Bergstrom, Christel A. S.
    [J]. PHARMACEUTICAL RESEARCH, 2017, 34 (09) : 1754 - 1772
  • [9] Mechanism-based selection of stabilization strategy for amorphous formulations: Insights into crystallization pathways
    Edueng, Khadijah
    Mahlin, Denny
    Larsson, Per
    Bergstrom, Christel A. S.
    [J]. JOURNAL OF CONTROLLED RELEASE, 2017, 256 : 193 - 202
  • [10] Physicochemical properties and stability of two differently prepared amorphous forms of simvastatin
    Graeser, Kirsten A.
    Strachan, Clare J.
    Patterson, James E.
    Gordon, Keith C.
    Rades, Thomas
    [J]. CRYSTAL GROWTH & DESIGN, 2008, 8 (01) : 128 - 135